Uci Continuing Education Certified Nursing Assistant School
The Trusted Standard in Research, Ethics, Compliance, and Safety Training
The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners.
Explore Our Featured Courses
- What's New
- Research
- Ethics
- Compliance
- Professional
- Other Offerings
QA/QI: Human Subjects Research
Featured New
Learn about QA/QI programs, how to conduct an internal audit, and strategies for using the findings.
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Disaster Response and Research Reactivation
Featured New
Provides strategies and information pertinent to disaster response and research reactivation.
Clery Act Training
Featured New
An in-depth review of the Clery Act and how higher education institutions can comply with applicable regulations.
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U.S. Department of Energy Interim Policy on Conflicts of Interest
Featured New
Provides an overview of the U.S. DOE's interim policy on conflicts of interest.
How to Conduct an Audit of a Ceded Study
Featured New
QA/QI professionals can learn to audit ceded studies for single IRB (sIRB) review.
Drones in Academia
Featured New
Explores the use of drones in research and the regulations and requirements researchers and administrators need to know.
Preparing for Success in Scholarly Publishing
Featured
Foundational course that orients and prepares learners to engage with the scholarly publication process in an informed way.
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Understanding 483s and Surviving Them
Featured New
Discusses steps that investigators and clinical sites can take to understand and respond to an FDA Form 483.
Managing Your Grants as Systems: A Guide for Grant Management Success
Featured New
Covers a systems approach to grant management and provides strategies for managing your team and your grant.
Preparing to Publish in Traditional and Hybrid Journals
Featured New
Covers key concepts in scholarly publishing and provides an overview of the publication process for both traditional and hybrid...
Data Management and Security for Student Researchers: An Overview
Featured
Covers the best practices of data management and security for graduate student researchers.
Protocol Development and Execution: Beyond a Concept
Featured New
An in-depth review of the development and execution of protocols.
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Race in Clinical Research: Ethics and IRB Decision Making
Featured
Explores the concept of race in clinical research and important ethical and regulatory questions.
Research Equity and the Part We Play
Featured New
Discusses ways to improve diversity and equity among clinical trial participants.
U.S. DoD Regulations & Requirements for Human Subject Research
Featured
Reviews DoD requirements and limitations for research.
CRISPR Genome Editing: Rewriting DNA and the Future of Humanity
Featured
Describes CRISPR genome editing, including its applications and ethical questions.
Privacy and Ethics for Connected and Automated Vehicles
Featured
An overview of connected and automated vehicles (CAVs) and the associated privacy and ethical challenges.
Undue Foreign Influence: Risks and Mitigations
Featured
Explore key ethical, export, security, intellectual property, and transparency requirements related to international engagement.
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Infection Prevention in Healthcare Settings
Featured New
Provides learners with a foundational understanding of infection prevention techniques.
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Laser Safety
Featured New
Meets the requirements of a general laser safety training program for research and medical institutions.
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General Laboratory Safety for Non-Laboratory Personnel
Featured New
Hazard awareness, communication, and safe practices for non-lab personnel working in and around laboratory facilities.
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FDA Inspections of GMP Facilities: How to Be Inspection Ready
Featured New
Discusses the FDA's approach to inspecting GMP facilities and the ways that facilities can prepare for inspections.
ClinicalTrials.gov Enforcement: An Update
Featured New
Explores recent FDA enforcement of FDAAA 801 and noncompliance pitfalls to avoid.
FCPA and University Research: What Faculty and Administrators Need to Know
Featured
Reviews FCPA as it relates to university research.
CRA Soft Skills, Time Management, and Effective Site Relationships
Featured New
Discusses the importance of CRA soft skills in building productive relationships with sites and sponsors.
Improving the Clinical Trial Participant's Experience
Featured New
Discusses ways that sponsors, sites, and clinical research organizations can transform the clinical trial experience.
Cost Allowability on Federally Sponsored Awards
Featured
A review of allowability of expenditures on federally supported projects.
IRB Review of Observational Research
Featured
Explores different types of observational research and provides best practices for IRB review.
Partnering with Technology Companies
Featured
Provides an overall approach to and best practices for partnering with technology companies to design and conduct research.
How to Effectively Manage a Research Administration Team
Featured New
Provides research administrators with strategies to build, improve, and retain employees.
CTrials by BRANY
Featured
CTrials helps grow sponsored research programs by taking on the many administrative challenges inherent in managing clinical trials.
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Protocol Builder
Featured
Protocol Builder is an online protocol writing and collaboration platform that also speed up your pre-review turnaround times.
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Tech Software
Featured
Tech Software a leading provider of SaaS compliance solutions for higher-education, academic medical centers, hospitals, government and biotech companies.
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The Network of Networks (N2)
Featured
N2 is a not-for-profit alliance of Canadian research networks and organizations working to enhance national clinical research capability and capacity.
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BIC Study Foundation
Featured
BIC Study Foundation is a resource for those who want to take CITI Program courses in Korean. They are a certified training provider by the Korean FDA/MAFRA for HRPP and ACU Programs.
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Meet A Few Of Our Expert Authors and Presenters
Our courses are built by over 150 highly qualified experts and rigorously peer reviewed to incorporate various perspectives and ensure accuracy, completeness, and overall quality.
Terry Adirim is Senior Associate Dean for Clinical Affairs, Professor of Pediatrics and Chair, Department of Integrated Medical Science at the Charles E. Schmidt College of Medicine where she is responsible for leading the the college's clinical enterprise.
Dr. Devino is Executive Director of Sponsored Programs at the University of Houston-Clear Lake. She holds a PhD in chemistry and served as a faculty member at two-year and four-year colleges before transitioning into full-time research development and administration.
Maya Nair, PhD, RBP, Director Biological Division of Environmental Health and Safety at UNT Health Science Center, Fort Worth, Texas, is an established Scientist, Educator and an Administrator. Dr. Nair is also the Biosafety and Radiation Safety Officer and reviewing official for UNTHSC's increased control program.
Margaret Rankovic is the Director for Content and Education. She is the lead developer for educational content in human subjects research, IRB administration, GCP, and more. Ms. Rankovic received her BA and MEd in research, statistics, and evaluation from the University of Virginia. She previously held her certified IRB professional credential for 9 years and has extensive knowledge of federal regulations, including FDA and HHS.
In Our Learners' Words
Julie S.
Assistant Professor & Postdoctoral Research Fellow
These courses were easy to access and succinct, which made a review of the Belmont Report key tenets, as well as the review of differences between practice and research, a focused and time efficient endeavor.
Myrene M.
Associate Faculty
The course materials are brief and clear. Such brevity and clarity are perfect for those who are busy with other duties at work and provide for a more friendly and less overwhelming task. I love the quizzes because I can learn from my mistakes. After submitting the quiz, the correct and wrong answers are explained. This reinforces learning.
Folasade A.
Student
I like the opportunity to be able to read/review CITI study notes at any time.
Motunrayo O.
Professor
Very educative course. It was insightful and informative. I learned and relearned a lot.
Courses Approved by a Top Academic CME Provider
CITI Program courses are approved for CME credits through the Albert Einstein Montefiore Continuing Professional Development Center (CPDC).
Albert Einstein College of Medicine-Montefiore Medical Center (Einstein) is accredited by the Joint Accreditation for Interprofessional Continuing Education to provide continuing education activities for healthcare professionals. Einstein is accredited to offer continuing education credit for the following professions: medicine, nursing, psychology, pharmacy, dentistry, optometry, social work, nutritional science, and athletic training.
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Recent News & Articles
Content Update News
New Webinar – How to Conduct an Audit of a Ceded Study
The presenter will outline steps to set your QA/QI program up for success, including available resources and tools to support the auditing of ceded studies.
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Blog
What CITI Program is Reading – October 18th, 2022
"What CITI Program is Reading" is our weekly blog series which highlights news articles curated by our staff and relevant to research, higher education, healthcare,...
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Upcoming Events
Free Live Webinar – Successfully Navigating Subrecipient Monitoring
Subrecipient monitoring is a federal requirement, but the regulations are often complex and confusing.
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Source: https://about.citiprogram.org/
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